ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.1827G>A (p.Val609=)

dbSNP: rs905577227
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV000515720 SCV000611842 uncertain significance Polycystic kidney disease no assertion criteria provided clinical testing

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